chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
132690341926903420GA28GENIChomozygous947934147
132690487426904875TC35GENIChomozygous947934148
132690502526905026TC37GENIChomozygous947934149
132690579726905798AG17GENIChomozygous947934150
132690605326906054AG25GENIChomozygous947934151
132690772226907723CT18GENIChomozygous947934152
132690806426908065TC21GENIChomozygous947934153
132690829026908291GA28GENIChomozygous947934154
132690888826908889CG24GENIChomozygous947934155
132690930926909310CT15GENIChomozygous947934156
132691024226910243CT25GENIChomozygous947934157
132691026926910270GC30GENIChomozygous947934158
132691093226910933GT11GENIChomozygous947934159
132691109026911091GA29GENIChomozygous947934160
132691133226911333GA30GENIChomozygous947934161
132691164826911649CT17GENIChomozygous947934162
132691182126911822CT19GENIChomozygous947934163
132691867226918673CT18GENIChomozygous947934164
132692003926920040AG20GENIChomozygous947934165
132692176126921762TC20GENIChomozygous947934166
132692184926921850AC27GENIChomozygous947934167
132692232126922322AT10GENIChomozygous947934168
132692238526922386AT11GENIChomozygous947934169
132692256126922562TC15GENIChomozygous947934170
132692257626922577CA18GENIChomozygous947934171
132692276726922768AG19GENIChomozygous947934172